Company Product Description Indication Status
Cosmo Artificial Intelligence Ltd./Cosmo Pharmaceuticals NV, of Dublin, and Medtronic plc, of Dublin GI Genius Computer-aided detection endoscopy module that uses artificial intelligence Assists clinicians in detecting lesions in the colon in real time during a colonoscopy U.S. FDA granted de novo clearance
Lucira Health Inc., of Emeryville, Calif. Lucira Check It At-home molecular test; available over the counter For the qualitative detection of SARS-CoV-2 U.S. FDA issued emergency use authorization
Masimo Corp., of Irvine, Calif. Radius PCG Portable, real-time capnograph with Bluetooth connectivity; connects with the Root patient monitoring and connectivity platform Measures, displays and monitors carbon dioxide partial pressure and respiratory rate during anesthesia, recovery and respiratory care Received 510(k) clearance from the U.S. FDA
Myhomedoc Ltd., of Rahanana, Israel Myhomedoc system Hand-held multisensor device that pairs with a smartphone For the remote examination of the mouth, throat, lungs, ears, heart, skin, abdomen, body temperature and oxygen saturation Received 510(k) clearance from the U.S. FDA
Thermo Fisher Scientific Inc., of Waltham, Mass. Applied Biosystems Taqpath COVID-19 Combo Kit Real-time RT-PCR test For the qualitative detection of nucleic acid from SARS-CoV-2 in upper respiratory specimens U.S. FDA expanded emergency use authorization to include the Thermo Fisher Scientific Amplitude platform


For more information about individual companies and/or products, see Cortellis.